Canonical Allele Identifier: CA2843744677

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47476681_47480794del , CM000664.2:g.47476681_47480794del	GRCh38
NC_000002.11:g.47703820_47707933del , CM000664.1:g.47703820_47707933del	GRCh37
NC_000002.10:g.47557324_47561437del	NCBI36
NG_007110.2:g.78558_82671del , LRG_218:g.78558_82671del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2210+110_2557del
ENST00000233146.7:c.2210+110_2557del
ENST00000543555.6:c.2012+110_2359del
ENST00000644092.1:c.*510+110_*857del
ENST00000644900.1:c.63+110_410del
ENST00000645339.1:c.2210+110_2557del
ENST00000645506.1:c.2210+110_2557del
ENST00000646415.1:c.2210+110_2557del
ENST00000233146.6:c.2210+110_2557del
ENST00000406134.5:c.2210+110_2557del
ENST00000543555.5:c.2012+110_2359del
ENST00000610696.4:c.*606+110_*953del
ENST00000613514.4:c.*750+110_*1097del
ENST00000617333.3:c.*976+110_*1323del
ENST00000617938.4:c.*1182+110_*1529del
ENST00000621359.2:c.2210+110_*123del
NM_000251.2:c.2210+110_2557del , LRG_218t1:c.2210+110_2557del
NM_001258281.1:c.2012+110_2359del
XM_005264332.2:c.2210+110_2557del
XM_011532867.1:c.2210+110_2557del
XR_939685.1:n.2282+110_2629del
XM_005264332.4:c.2210+110_2557del
XM_011532867.2:c.2210+110_2557del
XR_001738747.2:n.2272+110_2619del
XR_939685.2:n.2272+110_2619del
NM_000251.3:c.2210+110_2557del